PL2707003T3 - Krystaliczne sole amidu kwasu (4s,4as,5ar,12as)-4-dimetyloamino-3,10,12,12a-tetrahydroksy-7-[(metoksy(metylo)amino)metylo]-1,11-diokso- 1,4,4a,5,5a,6,11,12a-oktahydronaftaceno- 2-karboksylowego i sposoby ich stosowania - Google Patents

Krystaliczne sole amidu kwasu (4s,4as,5ar,12as)-4-dimetyloamino-3,10,12,12a-tetrahydroksy-7-[(metoksy(metylo)amino)metylo]-1,11-diokso- 1,4,4a,5,5a,6,11,12a-oktahydronaftaceno- 2-karboksylowego i sposoby ich stosowania

Info

Publication number
PL2707003T3
PL2707003T3 PL12782600T PL12782600T PL2707003T3 PL 2707003 T3 PL2707003 T3 PL 2707003T3 PL 12782600 T PL12782600 T PL 12782600T PL 12782600 T PL12782600 T PL 12782600T PL 2707003 T3 PL2707003 T3 PL 2707003T3
Authority
PL
Poland
Prior art keywords
methyl
naphthacene
tetrahydroxy
octahydro
dioxo
Prior art date
Application number
PL12782600T
Other languages
English (en)
Inventor
Catherine Coulter
Sean M Johnston
Farzaneh Seyedi
Original Assignee
Paratek Pharm Innc
Allergan Pharmaceuticals Int Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Paratek Pharm Innc, Allergan Pharmaceuticals Int Ltd filed Critical Paratek Pharm Innc
Publication of PL2707003T3 publication Critical patent/PL2707003T3/pl

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C237/00Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
    • C07C237/24Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a ring other than a six-membered aromatic ring of the carbon skeleton
    • C07C237/26Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a ring other than a six-membered aromatic ring of the carbon skeleton of a ring being part of a condensed ring system formed by at least four rings, e.g. tetracycline
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/10Anti-acne agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04Antibacterial agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C239/00Compounds containing nitrogen-to-halogen bonds; Hydroxylamino compounds or ethers or esters thereof
    • C07C239/08Hydroxylamino compounds or their ethers or esters
    • C07C239/20Hydroxylamino compounds or their ethers or esters having oxygen atoms of hydroxylamino groups etherified
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C309/00Sulfonic acids; Halides, esters, or anhydrides thereof
    • C07C309/01Sulfonic acids
    • C07C309/02Sulfonic acids having sulfo groups bound to acyclic carbon atoms
    • C07C309/03Sulfonic acids having sulfo groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
    • C07C309/04Sulfonic acids having sulfo groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton containing only one sulfo group
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/07Optical isomers
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13Crystalline forms, e.g. polymorphs
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2603/00Systems containing at least three condensed rings
    • C07C2603/02Ortho- or ortho- and peri-condensed systems
    • C07C2603/40Ortho- or ortho- and peri-condensed systems containing four condensed rings
    • C07C2603/42Ortho- or ortho- and peri-condensed systems containing four condensed rings containing only six-membered rings
    • C07C2603/44Naphthacenes; Hydrogenated naphthacenes
    • C07C2603/461,4,4a,5,5a,6,11,12a- Octahydronaphthacenes, e.g. tetracyclines

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Dermatology (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
PL12782600T 2011-05-12 2012-05-14 Krystaliczne sole amidu kwasu (4s,4as,5ar,12as)-4-dimetyloamino-3,10,12,12a-tetrahydroksy-7-[(metoksy(metylo)amino)metylo]-1,11-diokso- 1,4,4a,5,5a,6,11,12a-oktahydronaftaceno- 2-karboksylowego i sposoby ich stosowania PL2707003T3 (pl)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201161485179P 2011-05-12 2011-05-12
EP12782600.6A EP2707003B1 (en) 2011-05-12 2012-05-14 Crystalline salts of (4s,4as,5ar,12as)-4-dimethylamino-3,10,12,12a-tetrahydroxy-7-[(methoxy(methyl)amino)-methyl]-1,11-dioxo-1,4,4a,5,5a,6,11,12a-octahydro-naphthacene-2-carboxylic acid amide and methods of using the same
PCT/US2012/037838 WO2012155146A1 (en) 2011-05-12 2012-05-14 Crystalline salts of (4s,4as,5ar,12as)-4-dimethylamino-3,10,12,12a-tetrahydroxy-7-[(methoxy(methyl)amino)-methyl]-1,11-dioxo-1,4,4a,5,5a,6,11,12a-octahydro-naphthacene-2-carboxylic acid amide and methods of using the same

Publications (1)

Publication Number Publication Date
PL2707003T3 true PL2707003T3 (pl) 2019-11-29

Family

ID=47139728

Family Applications (1)

Application Number Title Priority Date Filing Date
PL12782600T PL2707003T3 (pl) 2011-05-12 2012-05-14 Krystaliczne sole amidu kwasu (4s,4as,5ar,12as)-4-dimetyloamino-3,10,12,12a-tetrahydroksy-7-[(metoksy(metylo)amino)metylo]-1,11-diokso- 1,4,4a,5,5a,6,11,12a-oktahydronaftaceno- 2-karboksylowego i sposoby ich stosowania

Country Status (14)

Country Link
US (4) US9255068B2 (pl)
EP (2) EP3574908B8 (pl)
JP (5) JP6574572B2 (pl)
CA (1) CA2835876C (pl)
DK (1) DK2707003T3 (pl)
ES (2) ES2739626T3 (pl)
HR (1) HRP20191295T8 (pl)
HU (1) HUE044536T2 (pl)
LT (1) LT2707003T (pl)
PL (1) PL2707003T3 (pl)
PT (1) PT2707003T (pl)
SI (1) SI2707003T1 (pl)
TR (1) TR201911086T4 (pl)
WO (1) WO2012155146A1 (pl)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8856782B2 (en) 2007-03-01 2014-10-07 George Mason Research Foundation, Inc. On-demand disposable virtual work system
US9098698B2 (en) 2008-09-12 2015-08-04 George Mason Research Foundation, Inc. Methods and apparatus for application isolation
ES2739626T3 (es) * 2011-05-12 2020-02-03 Paratek Pharm Innc Sales cristalinas de amida del ácido (4S,4aS,5aR,12aS)-4-dimetilamino-3,10,12,12a-tetrahidroxi-7-[(metoxi(metil)amino)-metil]-1,11-dioxo-1,4,4a,5,5a,6,11,12a-octahidro-naftacen-2-carboxílico y métodos de uso de las mismas
US9081959B2 (en) 2011-12-02 2015-07-14 Invincea, Inc. Methods and apparatus for control and detection of malicious content using a sandbox environment
JP2015517524A (ja) * 2012-05-14 2015-06-22 パラテック ファーマシューティカルズ インコーポレイテッド (4S,4aS,5aR,12aS)−4−ジメチルアミノ−3,10,12,12a−テトラヒドロキシ−7−[(メトキシ(メチル)アミノ)−メチル]−1,11−ジオキソ−1,4,4a,5,5a,6,11,12a−オクタヒドロ−ナフタセン−2−カルボン酸アミドの使用方法
HUE066360T2 (hu) 2016-10-19 2024-07-28 Tetraphase Pharmaceuticals Inc Eravaciklin kristályformái
CN111343991A (zh) * 2017-07-21 2020-06-26 阿尔米雷尔有限责任公司 非炎性病变的治疗
CA3095102A1 (en) * 2018-04-06 2019-10-10 Paratek Pharmaceuticals, Inc. Process for making sarecycline hydrochloride
EP4357798A4 (en) 2021-06-14 2025-05-21 Hioki E.E. Corporation SHORT-CIRCUIT DETECTION DEVICE AND SHORT-CIRCUIT DETECTION METHOD

Family Cites Families (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2990331A (en) 1956-11-23 1961-06-27 Pfizer & Co C Stable solutions of salts of tetracyclines for parenteral administration
US2980584A (en) 1957-10-29 1961-04-18 Pfizer & Co C Parenteral magnesium oxytetracycline acetic or lactic acid carboxamide vehicle preparation
US3062717A (en) 1958-12-11 1962-11-06 Pfizer & Co C Intramuscular calcium tetracycline acetic or lactic acid carboxamide vehicle preparation
US3165531A (en) 1962-03-08 1965-01-12 Pfizer & Co C 13-substituted-6-deoxytetracyclines and process utilizing the same
US3454697A (en) 1965-06-08 1969-07-08 American Cyanamid Co Tetracycline antibiotic compositions for oral use
NL6607516A (pl) 1966-05-31 1967-12-01
DE1767891C3 (de) 1968-06-28 1980-10-30 Pfizer Verfahren zur Herstellung von wäßrigen arzneilichen Lösungen für die parenterale, perorale und lokale Anwendung mit einem Gehalt an einem Tetracyclinderivat
US3957980A (en) 1972-10-26 1976-05-18 Pfizer Inc. Doxycycline parenteral compositions
DE2442829A1 (de) 1974-09-06 1976-03-18 Merck Patent Gmbh Tetracyclische verbindungen und verfahren zu ihrer herstellung
US4018889A (en) 1976-01-02 1977-04-19 Pfizer Inc. Oxytetracycline compositions
US4126680A (en) 1977-04-27 1978-11-21 Pfizer Inc. Tetracycline antibiotic compositions
JPH06256280A (ja) 1992-11-17 1994-09-13 Univ New York State 糖尿病における過度のコラーゲン架橋結合を阻害する非抗菌性化学修飾テトラサイクリンを含むテトラサイクリン
WO1995022529A1 (en) 1994-02-17 1995-08-24 Pfizer Inc. 9-(substituted amino)-alpha-6-deoxy-5-oxy tetracycline derivatives, their preparation and their use as antibiotics
US5789395A (en) 1996-08-30 1998-08-04 The Research Foundation Of State University Of New York Method of using tetracycline compounds for inhibition of endogenous nitric oxide production
US6277061B1 (en) 1998-03-31 2001-08-21 The Research Foundation Of State University Of New York Method of inhibiting membrane-type matrix metalloproteinase
ES2463457T3 (es) 2006-12-21 2014-05-28 Paratek Pharmaceuticals, Inc. Derivados de la tetraciclina para el tratamiento de infecciones bacterianas, virales y parasitarias
US8513223B2 (en) 2006-12-21 2013-08-20 Paratek Pharmaceuticals, Inc. Substituted tetracycline compounds for treatment of inflammatory skin disorders
CA2717703A1 (en) * 2008-03-05 2009-09-11 Paratek Pharmaceuticals, Inc. Minocycline compounds and methods of use thereof
TW202216656A (zh) * 2008-05-19 2022-05-01 美商Prtk Spv2公司 四環素化合物之甲苯磺酸鹽及同素異形體
ES2739626T3 (es) * 2011-05-12 2020-02-03 Paratek Pharm Innc Sales cristalinas de amida del ácido (4S,4aS,5aR,12aS)-4-dimetilamino-3,10,12,12a-tetrahidroxi-7-[(metoxi(metil)amino)-metil]-1,11-dioxo-1,4,4a,5,5a,6,11,12a-octahidro-naftacen-2-carboxílico y métodos de uso de las mismas
JP2015517524A (ja) * 2012-05-14 2015-06-22 パラテック ファーマシューティカルズ インコーポレイテッド (4S,4aS,5aR,12aS)−4−ジメチルアミノ−3,10,12,12a−テトラヒドロキシ−7−[(メトキシ(メチル)アミノ)−メチル]−1,11−ジオキソ−1,4,4a,5,5a,6,11,12a−オクタヒドロ−ナフタセン−2−カルボン酸アミドの使用方法

Also Published As

Publication number Publication date
ES2739626T3 (es) 2020-02-03
JP2019142867A (ja) 2019-08-29
CA2835876A1 (en) 2012-11-15
EP2707003B1 (en) 2019-05-01
US20200024223A1 (en) 2020-01-23
EP2707003A4 (en) 2014-11-12
JP2017132775A (ja) 2017-08-03
ES2985493T3 (es) 2024-11-06
JP2023093519A (ja) 2023-07-04
SI2707003T1 (sl) 2019-10-30
CA2835876C (en) 2020-04-14
JP6574572B2 (ja) 2019-09-11
HUE044536T2 (hu) 2019-10-28
EP3574908A1 (en) 2019-12-04
JP6876082B2 (ja) 2021-05-26
LT2707003T (lt) 2019-10-10
WO2012155146A1 (en) 2012-11-15
HRP20191295T8 (hr) 2020-02-07
US20130012480A1 (en) 2013-01-10
US20190040002A1 (en) 2019-02-07
TR201911086T4 (tr) 2019-08-21
EP2707003A1 (en) 2014-03-19
EP3574908B1 (en) 2024-07-31
PT2707003T (pt) 2019-08-05
HRP20191295T1 (hr) 2019-10-18
DK2707003T3 (da) 2019-08-05
US9255068B2 (en) 2016-02-09
JP2021098695A (ja) 2021-07-01
JP2014520077A (ja) 2014-08-21
EP3574908B8 (en) 2024-09-11
US20160200671A1 (en) 2016-07-14

Similar Documents

Publication Publication Date Title
HUE044536T2 (hu) A (4S,4aS,5aR,12aS)-4-dimetilamino-3,10,12,12a-tetrahidroxi-7-[(metoxi(metil)amino)-metil]- 1,11-dioxo-1,4,4a,5,5a,6,11,12a-oktahidro-naftacén-2-karbonsav amid és alkalmazási módszerei
CY1124874T1 (el) Διεργασια για την παρασκευη [(5-(3-χλωροφαινυλ)-3-υδροξυπυριδινο-2-καρβονυλ)-αμινο]οξικου οξεος απο 5-((3-χλωροφαινυλ)-3-χλωρο-πυριδιν-2-υλ)-νιτριλιο, και διεργασια για την παρασκευη παραγωγων 5-((αλογονοφαινυλ)-3-αλογονο-πυριδιν-2-υλ)-νιτριλιου
EP4406950A3 (en) Lfa-1 inhibitor and polymorph thereof
IL228979A (en) A rich compound and a pharmacist's application for her
ZA201307815B (en) N-(1,3,4-oxadiazol-2-yl)arylcarboxamides and use thereof as herbicides
IL230820A0 (en) N-[1-cyano-2-(phenyl)ethyl]-2-azabicyclo[1.2.2]heptane-3-carboxamide modified cathepsin c inhibitors
EP2796461A4 (en) PROCESS FOR THE PRODUCTION OF ICOTINIB AND ICOTINIB HYDROCHLORIDE AND INTERMEDIATES THEREOF
EP2526099A4 (en) IMPROVED METHOD FOR THE MANUFACTURE OF AMID INTERMEDIATE PRODUCTS AND ITS APPLICATION
SG11201403119TA (en) Mixtures of diphosphinic acids and dialkylphosphinic acids, a process for the preparation thereof and the use thereof
PL2565182T3 (pl) Nowa pochodna amidu i jej zastosowanie jako leku
ZA201301799B (en) Process for the preparation of pan-cdk inhibitors of the formula (i),and intermediates of the preparation
SG11201403150PA (en) Mixtures of diphosphinic acids and alkylphosphinic acids, a process for the preparation thereof and the use thereof
IL220665A0 (en) Pyruvamide compounds as inhibitors of dust time group 1 peptidase allergen and their use
ZA201403649B (en) [1,2,4]triazolopyridines and their use as phospodiesterase inhibitors
EP2849757A4 (en) PROCESS FOR USE OF (4S, 4AS, 5AR, 12AS -) - 4-DIMETHYLAMINO-3,10,12,12A-TETRAHYDROXY-7 - [(METHOXY (METHYL) AMINO) -METHYL] -1,11-DIOXO-1 , 4.4A, 5.5A, 6,11,12a-octahydro-naphthacene-2-carboxylic acid amide
PH12014500365A1 (en) An anti-termite biological formulation and a process for the preparation thereof
PL396622A1 (pl) Pochodne diestrów 4-metylotiofenylowych kwasów 1-amino-2-metylo-propanofosfonowych, sposób wytwarzania pochodnych diestrów 4-metylotiofenylowych kwasów 1-amino-2-metylo-propanofosfonowych oraz zastosowanie pochodnych diestrów 4-metylotiofenylowych kwasów 1-amino-2-metylo-propanofosfonowych
PL392175A1 (pl) Nowy propionian R-(-)-2-(5,5-dimetylocykloheks-2-en-1ylo) etylu i sposób jego otrzymywania
PL392173A1 (pl) Nowy octan R-(-)-2-(5,5-dimetylocykloheks-2-en-1-ylo)etylu i sposób jego otrzymywania
PL392169A1 (pl) Nowe propioniany 2-(4,4-dimetylocykloheks-2-en-1-ylo)etylu i sposób ich otrzymywania
PL392176A1 (pl) Nowe propioniany 2-(5,5-dimetylocykloheks-2-en-1-ylo)etylu i sposób ich otrzymywania
HK1191646A (en) Methods for the preparation of bendamustine
PL392170A1 (pl) Nowy ester etylowy kwasu S-(+)-(5,5-dimetylocykloheks-2-en-1-ylo)octowego i sposób jego otrzymywania
HUP1100239A2 (en) Novel process for the preparation of pharmaceutically active ingredient and the intermediates arose during the process
HUP1100238A2 (en) Novel process for the preparation of pharmaceutically active ingredient and the intermediates arose during the process